136 related articles for article (PubMed ID: 285339)
1. McArdle disease: phosphorylase activity in regenerating muscle fibers.
Mitsumoto H
Neurology; 1979 Feb; 29(2):258-62. PubMed ID: 285339
[TBL] [Abstract][Full Text] [Related]
2. McArdle disease: the mysterious appearance of phosphorylase activity in cells that ought to lack the genetic program. A fetal isoenzyme?
DiMauro S; Arnold S; Miranda A; Rowland LP
Trans Am Neurol Assoc; 1977; 102():112-5. PubMed ID: 278321
[No Abstract] [Full Text] [Related]
3. McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture--a fetal isoenzyme.
DiMauro S; Arnold S; Miranda A; Rowland LP
Ann Neurol; 1978 Jan; 3(1):60-6. PubMed ID: 418736
[TBL] [Abstract][Full Text] [Related]
4. Characterization of glycogen phosphorylase isoenzymes present in cultured skeletal muscle from patients with McArdle's disease.
Sato K; Imai F; Hatayama I; Roelofs RI
Biochem Biophys Res Commun; 1977 Sep; 78(2):663-8. PubMed ID: 269730
[No Abstract] [Full Text] [Related]
5. Phosphorylation of McArdle phosphorylase induces activity.
Cerri CG; Willner JH
Proc Natl Acad Sci U S A; 1981 May; 78(5):2688-92. PubMed ID: 6265901
[TBL] [Abstract][Full Text] [Related]
6. A new variant of late-onset myophosphorylase deficiency.
Kost GJ; Verity MA
Muscle Nerve; 1980; 3(3):195-201. PubMed ID: 6929403
[TBL] [Abstract][Full Text] [Related]
7. Phosphorylase isoenzymes in normal and myophosphorylase-deficient human heart.
Miranda AF; Nette EG; Hartlage PL; DiMauro S
Neurology; 1979 Nov; 29(11):1538-41. PubMed ID: 291791
[TBL] [Abstract][Full Text] [Related]
8. [Glycogenosis type V of adults: muscle phosphorylase deficiency].
Coll Cantí J; Illa I; Beleta J; Anglada A; Pradas J; González Sastre F; Grau Veciana JM; Gella FJ
Med Clin (Barc); 1986 Mar; 86(8):335-8. PubMed ID: 3458989
[No Abstract] [Full Text] [Related]
9. Histochemical phosphorylase activity in regenerating muscle fibers from myophosphorylase-deficient patients.
Roelofs RI; Engel WK; Chauvin PB
Science; 1972 Sep; 177(4051):795-7. PubMed ID: 4506147
[TBL] [Abstract][Full Text] [Related]
10. Histochemical and biochemical studies in a patient with myophosphorylase deficiency.
Tachi N; Sasaki K; Tachi M; Sugie H
Eur Neurol; 1990; 30(1):52-5. PubMed ID: 2298228
[TBL] [Abstract][Full Text] [Related]
11. [Morphological and biochemical studies on glycogenosis type V (McArdle) (author's transl)].
Pongratz D; Schaub J; Koppenwallner C; Hübner G
Klin Wochenschr; 1981 Sep; 59(18):1053-9. PubMed ID: 6795385
[TBL] [Abstract][Full Text] [Related]
12. Sodium valproate increases the brain isoform of glycogen phosphorylase: looking for a compensation mechanism in McArdle disease using a mouse primary skeletal-muscle culture in vitro.
de Luna N; Brull A; Guiu JM; Lucia A; Martin MA; Arenas J; Martí R; Andreu AL; Pinós T
Dis Model Mech; 2015 May; 8(5):467-72. PubMed ID: 25762569
[TBL] [Abstract][Full Text] [Related]
13. Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease.
Howell JM; Walker KR; Creed KE; Dunton E; Davies L; Quinlivan R; Karpati G
Neuromuscul Disord; 2014 Feb; 24(2):167-77. PubMed ID: 24309536
[TBL] [Abstract][Full Text] [Related]
14. In McArdle disease, phosphorylase deficiency is the tip of an iceberg.
Willner JH; Cerri CG; Wood DS; Ponzetto-Zimmerman C; Reydel PM
Trans Am Neurol Assoc; 1981; 106():208-9. PubMed ID: 6294950
[No Abstract] [Full Text] [Related]
15. McArdle's disease--what limit to the age of onset?
Hewlett RH; Gardner-Thorpe C
S Afr Med J; 1978 Jan; 53(2):60-3. PubMed ID: 273990
[TBL] [Abstract][Full Text] [Related]
16. Adenovirus-mediated delivery into myocytes of muscle glycogen phosphorylase, the enzyme deficient in patients with glycogen-storage disease type V.
Baqué S; Newgard CB; Gerard RD; Guinovart JJ; Gómez-Foix AM
Biochem J; 1994 Dec; 304 ( Pt 3)(Pt 3):1009-14. PubMed ID: 7818463
[TBL] [Abstract][Full Text] [Related]
17. Research on molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). Use of new protein mapping and immunological techniques.
Daegelen-Proux D; Kahn A; Marie J; Dreyfus JC
Ann Hum Genet; 1981 May; 45(2):113-20. PubMed ID: 6797345
[TBL] [Abstract][Full Text] [Related]
18. Myophosphorylase deficiency: two different molecular etiologies.
Feit H; Brooke MH
Neurology; 1976 Oct; 26(10):963-7. PubMed ID: 1066528
[TBL] [Abstract][Full Text] [Related]
19. [McArdle's disease (muscular phosphorylase deficiency)].
Schollmeyer P; Nolte J; Meisel D; Dichgans J; Jerusalem F
Verh Dtsch Ges Inn Med; 1977 Apr 17-21; 83():1277-80. PubMed ID: 274025
[No Abstract] [Full Text] [Related]
20. Congenital myopathy due to phosphorylase deficiency.
Cornelio F; Bresolin N; DiMauro S; Mora M; Balestrini MR
Neurology; 1983 Oct; 33(10):1383-5. PubMed ID: 6577313
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]